Top tips for nausea?: Although not yet... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

Top tips for nausea?

Fio1331 profile image
2 Replies

Although not yet formally diagnosed, my GP and I are both pretty certain that having ruled out everything else, I have CFS/ME.

Aside from the overall malaise, weakness etc, which has meant I've been pretty much housebound since June, my worst specific symptom is nausea.

On my worst days I just feel so sick all the time, and I have very disturbed sleep as I wake several times in the night with sudden surges of extreme nausea. It's ghastly.

I'm sure other people must have this too - are there any tips you can pass on for dealing with this? I'm not on any meds for my fatigue condition (yet!).

Thanks,

F

Written by
Fio1331 profile image
Fio1331
To view profiles and participate in discussions please or .
2 Replies

Hi Fio. I tend to use Valoid on a regular basis. Its been a struggle but I have managed to put on a stone and a half this past year after some dramatic weight loss using those.

Also cannabis can be used if you are in a place where you can get it as can ginger.

Hope that helps. take care.

Fio1331 profile image
Fio1331 in reply to

Thanks v much. I'd forgotten ginger was good - we actually already have a ginger tea in the cupboard so I'll start with that!

Not what you're looking for?

You may also like...

New to site, nervous. Tips on exercise, weight loss and working day tips needed

Hello I'm new to this site, was diagnosed last January after 2 years of tests following my 3rd...
beckyk1987 profile image

What IS fatigue?!

Hello all I'm not being facetious, I'm genuinely curious to try to understand my (potential/not yet...
Fio1331 profile image

Waiting for diagnosis

Hi, It's been 12 months and i am still waiting for a diagnosis for my tiredness. It started in...
HannahCB92 profile image

ME Flare ups and sleep problems

Hi everyone, I'm currently undiagnosed with CFS as I haven't had symptoms for 3/4 months yet.I've...

At my wits end with CFS

I have only had CFS for around 9 months but am already at my wits end. It was bought on by...

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.